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rs267607106

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(C;C) 0 common in clinvar
Make rs267607106(C;G)
Make rs267607106(G;G)
ReferenceGRCh38 38.1/141
Chromosome7
Position35249968
GeneTBX20
is asnp
is mentioned by
dbSNPrs267607106
ebirs267607106
HLIrs267607106
Exacrs267607106
Varsomers267607106
Maprs267607106
PheGenIrs267607106
hapmaprs267607106
1000 genomesrs267607106
hgdprs267607106
ensemblrs267607106
gopubmedrs267607106
geneviewrs267607106
scholarrs267607106
googlers267607106
pharmgkbrs267607106
gwascentralrs267607106
openSNPrs267607106
23andMers267607106
23andMe allrs267607106
SNP Nexus

SNPshotrs267607106
SNPdbers267607106
MSV3drs267607106
GWAS Ctlgrs267607106
Max Magnitude0
ClinVar
Risk rs267607106(G;G)
Alt rs267607106(G;G)
Reference rs267607106(C;C)
Significance Pathogenic
Disease Atrial septal defect 4
Variation info
Gene TBX20
CLNDBN Atrial septal defect 4
Reversed 1
HGVS NC_000007.13:g.35289580G>C
CLNSRC OMIM Allelic Variant
CLNACC RCV000004897.2,